A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv951525



Internal ID16953712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:69413985..69438984hg38UCSC Ensembl
Outerchr9:72028901..72053900hg19UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg3825000
hg1925000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2996904
SamplesBILGI_BIOE
Known GenesAPBA1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv951525
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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